ChemInform Abstract: Recent Advances in the Synthesis of Nitrogen-Containing Heterocycles by Transition Metal Catalyzed Reactions

ChemInform ◽  
2010 ◽  
Vol 41 (8) ◽  
Author(s):  
Elena Borsini ◽  
Gianluigi Broggini
2017 ◽  
Vol 15 (40) ◽  
pp. 8483-8492 ◽  
Author(s):  
Long Li ◽  
Tong-De Tan ◽  
Ying-Qi Zhang ◽  
Xin Liu ◽  
Long-Wu Ye

In this review, recent progress in the transition-metal-catalyzed formal annulations of alkynes with isoxazoles for the efficient synthesis of N-heterocycles is discussed.


Synthesis ◽  
2021 ◽  
Author(s):  
Tom G. Driver ◽  
Wrickban Mazumdar

AbstractRecent catalytic methods to construct medium-sized lactams­ and partially saturated benzazepines and their derivatives are surveyed. The review is divided into the following sections:1 Introduction2 Non-Transition-Metal-Catalyzed Reactions2.1 Beckmann Rearrangement2.2 Non-Beckmann Rearrangement Reactions2.3 Multicomponent reactions3 Transition-Metal-Catalyzed Reactions3.1 Gold-Catalyzed Reactions to Access Medium-Sized N-Hetero­cycles3.2 Reactions Involving a Metal η3-Complex Catalytic Intermediate3.3 Transition-Metal-Catalyzed Reactions of Strained Cycloalkanes4 Conclusions


Author(s):  
Mohini Shrestha ◽  
Xianqing Wu ◽  
Wenyi Huang ◽  
Jingping Qu ◽  
Yifeng Chen

The development of carbamoyl chlorides as synthons for various amide-containing molecules and heterocycles have been summarized and discussed in this review article. Carbamoyl chlorides can participate in a diverse range...


2020 ◽  
Vol 7 (8) ◽  
pp. 1022-1060 ◽  
Author(s):  
Wenbo Ma ◽  
Nikolaos Kaplaneris ◽  
Xinyue Fang ◽  
Linghui Gu ◽  
Ruhuai Mei ◽  
...  

This review summarizes recent advances in C–S and C–Se formations via transition metal-catalyzed C–H functionalization utilizing directing groups to control the site-selectivity.


2020 ◽  
Vol 24 (3) ◽  
pp. 231-264 ◽  
Author(s):  
Kevin H. Shaughnessy

Phosphines are widely used ligands in transition metal-catalyzed reactions. Arylphosphines, such as triphenylphosphine, were among the first phosphines to show broad utility in catalysis. Beginning in the late 1990s, sterically demanding and electronrich trialkylphosphines began to receive attention as supporting ligands. These ligands were found to be particularly effective at promoting oxidative addition in cross-coupling of aryl halides. With electron-rich, sterically demanding ligands, such as tri-tertbutylphosphine, coupling of aryl bromides could be achieved at room temperature. More importantly, the less reactive, but more broadly available, aryl chlorides became accessible substrates. Tri-tert-butylphosphine has become a privileged ligand that has found application in a wide range of late transition-metal catalyzed coupling reactions. This success has led to the use of numerous monodentate trialkylphosphines in cross-coupling reactions. This review will discuss the general properties and features of monodentate trialkylphosphines and their application in cross-coupling reactions of C–X and C–H bonds.


2021 ◽  
Vol 17 ◽  
Author(s):  
Austin Pounder ◽  
Angel Ho ◽  
Matthew Macleod ◽  
William Tam

: Oxabenzonorbornadiene (OBD) is a useful synthetic intermediate which can be readily activated by transition metal complexes with great face selectivity due to its dual-faced nature and intrinsic angle strain on the alkene. To date, the understanding of transition-metal catalyzed reactions of OBD itself has burgeoned; however, this has not been the case for unsymmetrical OBDs. Throughout the development of these reactions, the nature of C1-substituent has proven to have a profound effect on both the reactivity and selectivity of the outcome of the reaction. Upon substitution, different modes of reactivity arise, contributing to the possibility of multiple stereo-, regio-, and in extreme cases, constitutional isomers which can provide unique means of constructing a variety of synthetically useful cyclic frameworks. To maximize selectivity, an understanding of bridgehead substituent effects is crucial. To that end, this review outlines hitherto reported examples of bridgehead substituent effects on the chemistry of unsymmetrical C1-substituted OBDs.


2021 ◽  
Vol 444 ◽  
pp. 214065
Author(s):  
Priyanka Chakraborty ◽  
Rajib Mandal ◽  
Nidhi Garg ◽  
Basker Sundararaju

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